A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv362n206



Internal ID22755666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194515252..194559177hg38UCSC Ensembl
chr3:194235981..194279906hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3843926
hg1943926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6139969, nsv5449071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv362n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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